NDC 57237-042 – Valacyclovir Hydrochloride
Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC57237-042
Product details
- Brand name
- Valacyclovir Hydrochloride
- Generic name
- Valacyclovir Hydrochloride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090682
- Marketed since
- May 24, 2010
- Listing expires
- December 31, 2027
- Pharmacologic class
- Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor
Active ingredients
- Valacyclovir Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Valacyclovir Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 57237-042-05 | 500 TABLET, FILM COATED in 1 BOTTLE (57237-042-05) | May 24, 2010 |
| 57237-042-30 | 30 TABLET, FILM COATED in 1 BOTTLE (57237-042-30) | May 24, 2010 |
| 57237-042-90 | 90 TABLET, FILM COATED in 1 BOTTLE (57237-042-90) | May 24, 2010 |
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